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. 2004 Aug;78(16):8812–8823. doi: 10.1128/JVI.78.16.8812-8823.2004

TABLE 2.

Characterization of clinical samples

Virus or animal no.a Sampleb Titer (SK6/Macr)c % Inhibition by heparind Plaque sizee
CoBrB 476S SK6 4.5/6.8 0 Large
5012 Tonsil 6.0/7.1 40 Large
Kidney 5.7/6.9 40 Large
Blood 6.3/6.6 65 Large
CoBrB 476S/C1.1.1 (E2-p7-pNS2-3′) 5016 SK6 4.0/6.3 5 Large
Tonsil 6.4/7.3 55 Large
Kidney 5.0/6.6 55 Large
Blood 4.9/5.7 80 Large
C1.1.1/CoBrB SK6 6.7/5.9 100 Small
5020 Tonsil NDf ND ND
Kidney ND ND ND
Blood 1.0/2.3 100 Small
CoBrB/C1.1.1 (Npro′-C-Erns-E1) 5024 SK6 6.3/6.2 100 Small
Tonsil 7.5/6.9 95 Small
Kidney 5.5/4.8 100 Small
Blood 4.3/4.4 100 Small/largeg
a

In vitro (SK6)- or in vivo-generated (animal number) virus.

b

Tonsil and kidney samples were prepared postmortem. EDTA-treated blood, taken at day 14 p.i., was tested.

c

Titers (log10 PFU per milliliter) were measured in a plaque assay using SK6 cells or lung macrophages (Macr).

d

Percent inhibition of infection of SK6 cells by 225 μg of heparin per ml.

e

Relative plaque size observed after 2 days of growth in a plaque assay using SK6 cells. Cells were not treated with heparin.

f

ND, not determined.

g

In the blood from this animal, approximately 1:100 plaques was a large-plaque variant.